# GEMCITABINE

NDC: 0409-0187
Generic name: GEMCITABINE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20101115

FDA application: ANDA079183

## Active ingredients

- GEMCITABINE HYDROCHLORIDE: 38 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-0187"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-0187
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a625c92b-c569-4b98-8d2e-2b3f5e12b34f